Research Coordinator I

About the role

The research coordinator I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes recruitment, screening, enrollment, randomization and management of the patient per the research protocol. The research coordinator I will collect data, patient reported outcomes, and questionnaires as required. The research coordinator I may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. The research coordinator I will collaborate with research coordinators, data managers and regulatory specialists. Other duties may be performed as assigned. Travel may be required.

Responsibilities

• Understands and knowledgeable of policies, procedures, and regulations governing human subject?s research and incorporates them in securing approval for and the conduct of research.
• Implements, coordinates, manages and reports to the Institutional Review Board (IRB).
• Implements, coordinates and manages clinical research operations.
• Establishs and maintains communication with Investigators, research staff, study sponsors, research participants and their family members, and representatives of professional organizations associated with the conduct of the research.
• Serves as an advocate for the human subjects by establishing and maintaining compliance in the conduct of the research protocol.
• Actively identifies and participates in training, education and development activities to improve own knowledge and performance to sustain and enhance professional development.
• Completes assigned goals.

Requirements

• Experience: Minimum Required 2 years Lab, Medical and/or Research background; Preferred/Desired 2 Years Research Experience.
• Education: Minimum Required High School Diploma; Preferred/Desired Associate’s Degree or equivalent experience.
• Training: Minimum Required Knowledge of Medical Terminology.

Skills

• Computer skills: MS Word.
• Excellent Organizational Skills.
• Detail Oriented.
• Experience with EMR and Clinical Trials Management System.
• BLS licensure (preferred).